Source: European Medicines Agency (EU) Revision Year: 2023 Publisher: KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
Darunavir Krka 400 mg film-coated tablets.
Darunavir Krka 800 mg film-coated tablets.
Pharmaceutical Form |
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Film-coated tablet (tablet). Darunavir Krka 400 mg film-coated tablets: Yellowish brown, oval, biconvex film-coated tablets, engraved with a mark S1 on one side. Tablet dimension: 17 × 8.5 mm. Darunavir Krka 800 mg film-coated tablets: Brownish red, oval, biconvex film-coated tablets, engraved with a mark S3 on one side. Tablet dimension: 20 × 10 mm. |
Darunavir Krka 400 mg film-coated tablets: Each film-coated tablet contains 400 mg darunavir.
Darunavir Krka 800 mg film-coated tablets: Each film-coated tablet contains 800 mg darunavir.
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Darunavir |
Darunavir is an inhibitor of the dimerisation and of the catalytic activity of the HIV-1 protease (KD of 4.5 × 10-12 M). It selectively inhibits the cleavage of HIV encoded Gag-Pol polyproteins in virus infected cells, thereby preventing the formation of mature infectious virus particles. |
List of Excipients |
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Tablet core: Cellulose, microcrystalline Film coating: Poly(vinyl alcohol) |
400 mg film-coated tablets:
Bottle (HDPE), child resistant tamper evident PP closure with a desiccant:
800 mg film-coated tablets:
Bottle (HDPE), child resistant tamper evident PP closure with a desiccant:
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
400 mg film-coated tablets:
30 film-coated tablets: EU/1/17/1249/001
60 film-coated tablets: EU/1/17/1249/002
90 film-coated tablets: EU/1/17/1249/003
180 film-coated tablets: EU/1/17/1249/004
800 mg film-coated tablets:
30 film-coated tablets: EU/1/17/1249/009
90 film-coated tablets: EU/1/17/1249/010
Date of first authorisation: 26 January 2018
Date of latest renewal: 9 November 2022
Drug | Countries | |
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DARUNAVIR | Nigeria |
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